Canonical Allele Identifier: CA1525089265
Gene: LINC02145 HGNC NCBI

Linked Data

dbSNP Id: rs1737040413

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.6324082T>G , CM000667.2:g.6324082T>G GRCh38
NC_000005.9:g.6324195T>G , CM000667.1:g.6324195T>G GRCh37
NC_000005.8:g.6377195T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_028351.1:n.144-11366A>C